# W.L. Gore & Associates

- Location (FDA's records): Flagstaff, AZ
- FDA decisions: 3 (2005–2012): 3 510(k) clearances
- Product codes: NTE (1), FTL (1), DSY (1)
- Predicates its devices cite: 7 (0 its own); citations of its devices by later devices: 0 (0 its own)
- Recalls linked to its devices: 0 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Firms whose devices it cites most
- W. L. Gore & Associates, Inc.: 4 (https://510kreport.com/company/w-l-gore-associates)
- Atrium Medical Corp.: 2 (https://510kreport.com/company/atrium-medical)
- Guidant Corp.: 1 (https://510kreport.com/company/guidant)

## Recent decisions
- K120480: Gore (R) Embolic Filter (Mar 16, 2012)
- K093934: Gore Hybrid Vascular Graft (Mar 17, 2010)
- K053202: Gore Seamguard Bioabsorbable Staple Line Reinforcement Material (Dec 7, 2005)

Source page: https://510kreport.com/company/wl-gore-associates